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rs2274224

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2274224(C;C)
Make rs2274224(C;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position94279840
GenePLCE1, PLCE1-AS1
is asnp
is mentioned by
dbSNPrs2274224
dbSNP (old)rs2274224
ClinGenrs2274224
ebirs2274224
HLIrs2274224
Exacrs2274224
Gnomadrs2274224
Varsomers2274224
Maprs2274224
PheGenIrs2274224
Biobankrs2274224
1000 genomesrs2274224
hgdprs2274224
ensemblrs2274224
gopubmedrs2274224
geneviewrs2274224
scholarrs2274224
googlers2274224
pharmgkbrs2274224
gwascentralrs2274224
openSNPrs2274224
23andMers2274224
23andMe allrs2274224
SNP Nexus

SNPshotrs2274224
SNPdbers2274224
MSV3drs2274224
GWAS Ctlgrs2274224
GMAF0.4683
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 23688607] Novel functional variants locus in PLCE1 and susceptibility to esophageal squamous cell carcinoma: Based on published genome-wide association studies in a central Chinese population


[PMID 16385451OA-icon.png] A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.


ClinVar
Risk rs2274224(A;A) rs2274224(C;C)
Alt rs2274224(A;A) rs2274224(C;C)
Reference Rs2274224(G;G)
Significance Non-pathogenic
Disease not specified Nephrotic syndrome
Variation info
Gene PLCE1 PLCE1-AS1
CLNDBN not specified Nephrotic syndrome
Reversed 0
HGVS NC_000010.10:g.96039597G>C
CLNSRC
CLNACC RCV000254331.1, RCV000394591.1,